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Good Clinical Practices (Final With Links)

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Good Clinical Practices

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Introduction: Good Clinical Practices
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Who Can Be An Investigator?
Good Clinical Practice mandates: ,[object Object],[object Object],[object Object],[object Object]
Good Clinical Practice mandates: ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Good Clinical Practice mandates: ,[object Object],[object Object],[object Object],[object Object],[object Object]
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Rules of Good Clinical Practice ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
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Test Your Knowledge ,[object Object],[object Object],[object Object]
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IRB Approval ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
CONSENT Subjects must be fully informed about the study. ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
ASSENT For Children ,[object Object]
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[object Object],[object Object],[object Object],You may have other reporting responsibilities (e.g. study sponsor, funding agency, NIH, etc.). You should learn what these are prior to initiating the study.
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Scenario ,[object Object],[object Object],[object Object],[object Object],[object Object]
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[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Test – Good Clinical Practices
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Good Clinical Practices (Final With Links)

  • 1. Introduction: Good Clinical Practices
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